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PharmaCM CT 2.0 to Help Pharma Manage Multinational Registries
Date:8/20/2013

NEW YORK, Aug. 20, 2013 /PRNewswire/ -- With the life sciences R&D industry undergoing a "major shift around modernization," Deloitte Analytics LLC is releasing PharmaCM CT 2.0, a solution that gives pharmaceutical and biotech companies one system for managing the clinical trial application process in both the United States and Europe.

PharmaCM CT 2.0 automates much of the activity involved in initiating clinical trials on the U.S. and European registries and in complying with ongoing disclosure and publishing requirements. It's an upgrade from PharmaCM CT 1.0 in that it supports the European Clinical Trial Database (EudraCT) in addition to its U.S. counterpart, ClinicalTrials.gov.

"Today's pharma and biotech companies play on a global stage, so they need solutions that do the same," said Thomas Wicks, general manager, Deloitte Analytics LLC and PharmaCM business leader. "Using a single platform to manage more of a firm's global trial activity will reduce time training staff and doing manual procedures."

According to Matthew Hudes, managing principal, Deloitte Consulting LLP and leader of Deloitte's biotechnology industry practice, products like PharmaCM CT 2.0 reflect a broader transformation underway working to modernize the R&D process.

"One of the promising trends in life sciences today is how drug and device development is adopting innovative process improvements – techniques that have greatly enhanced productivity in other industries," said Hudes. "PharmaCM CT 2.0 is an example of how pharma and biotech may be able to utilize these capabilities to substantially improve the R&D process."

Wicks said PharmaCM CT 2.0's functionality includes managing disclosure workflows, accepting data from multiple sources and tracking compliance dates. He also noted that it's
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SOURCE Deloitte Analytics LLC
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